Variant report

Variant	rs74022953
Chromosome Location	chr15:73656129-73656130
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:73655148..73657136-chr15:73673095..73675743,2	MCF-7	breast:
2	chr15:73653780..73658080-chr15:73658214..73662015,4	MCF-7	breast:
3	chr15:73644236..73646707-chr15:73654273..73657085,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000138622	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs74022959	1.00[AFR][1000 genomes]
rs74022961	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv904343	chr15:73396760-73775043	Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv457202	chr15:73612377-73680301	Bivalent Enhancer Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv569949	chr15:73612377-73680301	Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv524049	chr15:73612833-73680301	Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:73651200-73659000	Weak transcription	Pancreas	Pancrea
2	chr15:73651600-73658600	Enhancers	Right Ventricle	heart
3	chr15:73653200-73657200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr15:73653600-73656200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr15:73653600-73656400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr15:73653800-73656200	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr15:73654000-73656600	Enhancers	H1 Cell Line	embryonic stem cell
8	chr15:73654200-73656200	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr15:73654200-73656400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr15:73654200-73656400	Weak transcription	Fetal Brain Male	brain
11	chr15:73654600-73657800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr15:73655000-73656200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr15:73655000-73656400	Enhancers	Right Atrium	heart
14	chr15:73655400-73657000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr15:73655400-73657200	Enhancers	Fetal Heart	heart
16	chr15:73655600-73657800	Weak transcription	Left Ventricle	heart
17	chr15:73655800-73656200	Enhancers	H9 Cell Line	embryonic stem cell
18	chr15:73655800-73658200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr15:73655800-73658200	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr15:73656000-73656200	Bivalent Enhancer	Fetal Brain Female	brain
21	chr15:73656000-73657200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr15:73656000-73657600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr15:73656000-73657800	Weak transcription	HUES48 Cell Line	embryonic stem cell

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